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90 积分 2024-11-20 加入
胎儿肢体发育缺陷的超声产前筛查、诊断和遗传咨询专家共识(2025版)
2个月前
已完结
Knowledge, acceptance, and willingness to pay for expanded carrier screening among obstetric patients in China: Implications for genetic counseling practice
2个月前
已完结
[Expert consensus on clinical genetic counseling of α-thalassemia gene analysis]
2个月前
已完结
High prevalence of neonatal presentation in Korean patients with citrullinemia type 1, and their shared mutations
3个月前
已完结
Clinical utility of expanded carrier screening in the preconception and prenatal population: A Chinese cohort study
4个月前
已完结
Clinical implications of expanded carrier screening for pregnancy-related care and individual health
4个月前
已完结
Integrated Genotyping Strategies for Uncovering Detailed Haplotype Structures and Characterization of DMD Duplications
4个月前
已完结
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
4个月前
已完结
Single-center experience using reflex-targeted next-generation sequencing at diagnosis of squamous cell lung carcinoma in daily practice
5个月前
已关闭
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity
1年前
已完结
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